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Merck
모든 사진(1)

문서

91018

Supelco

(S)-NIFE

for chiral derivatization, ≥98.0%

동의어(들):

N-(4-Nitrophenoxycarbonyl)-L-phenylalanine 2-methoxyethyl ester

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About This Item

실험식(Hill 표기법):
C19H20N2O7
CAS Number:
Molecular Weight:
388.37
MDL number:
UNSPSC 코드:
12000000
PubChem Substance ID:

Grade

for chiral derivatization

분석

≥98.0% (HPLC)
≥98.0%

형태

powder

SMILES string

COCCOC(=O)[C@H](Cc1ccccc1)NC(=O)Oc2ccc(cc2)[N+]([O-])=O

InChI

1S/C19H20N2O7/c1-26-11-12-27-18(22)17(13-14-5-3-2-4-6-14)20-19(23)28-16-9-7-15(8-10-16)21(24)25/h2-10,17H,11-13H2,1H3,(H,20,23)/t17-/m0/s1

InChI key

ZSOUYIBYVUBOGT-KRWDZBQOSA-N

기타 정보

New chiral derivatizing agent for amino acid analysis by HPLC; derivatization of secondary amino acids

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

Sonika Sethi et al.
Biomedical chromatography : BMC, 34(1), e4730-e4730 (2019-10-28)
LC separation of biologically and pharmaceutically important enantiomers (from racemic or non-racemic mixtures) remains a subject of importance. The present review article deals with the liquid chromatographic enantioseparation of chiral selective serotonin reuptake inhibitors (SSRIs), namely citalopram, paroxetine, sertraline and
E. Olajos et al.
Chromatographia, 54, 77-77 (2001)
Cecilia Barbas-Bernardos et al.
Journal of chromatography. A, 1611, 460598-460598 (2019-10-20)
In the nutrition field, there is a lack of understanding about the impact that dietary chiral composition may have on health, especially regarding cooked meals. Chiral amino acids (AAs) are naturally present in food and their proportion may vary quite
A. Peter et al.
Chromatographia, 52, 821-821 (2000)
Antal Péter et al.
Journal of chromatography. A, 948(1-2), 283-294 (2003-07-02)
A new chiral derivatizing agent, (S)-N-(4-nitrophenoxycarbonyl)phenylalanine methoxyethyl ester, (S)-NIFE, was applied for the high-performance liquid chromatographic separation of enantiomers of 19 unnatural secondary amino acids: proline, pipecolic acid analogues, piperazine-2-carboxylic acid, morpholine-3-carboxylic acid, thiomorpholine-3-carboxylic acid and analogues containing the 1,2,3,4-tetrahydroisoquinoline

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